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Common Variants of the Genes Encoding Erythropoietin and Its Receptor Modulate Cognitive Performance in Schizophrenia.
- Published in:
- Molecular Medicine, 2012, v. 18, n. 6, p. 1029, doi. 10.2119/molmed.2012.00190
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- Publication type:
- Article
CALHM1 P86L Polymorphism Modulates CSF Aβ Levels in Cognitively Healthy Individuals at Risk for Alzheimer's Disease.
- Published in:
- Molecular Medicine, 2011, v. 17, n. 9/10, p. 974, doi. 10.2119/molmed.2011.00154
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- Publication type:
- Article
Association of catechol-O-methyltransferase variants with loudness dependence of auditory evoked potentials.
- Published in:
- Human Psychopharmacology: Clinical & Experimental, 2008, v. 23, n. 2, p. 115, doi. 10.1002/hup.906
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- Publication type:
- Article
Atypical Parkinsonism due to a D202N Gerstmann-Sträussler-Scheinker prion protein mutation: First in vivo diagnosed case.
- Published in:
- 2013
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- Publication type:
- Journal Article
Atypical Parkinsonism due to a D202 N Gerstmann- Sträussler- Scheinker prion protein mutation: First in vivo diagnosed case.
- Published in:
- Movement Disorders, 2013, v. 28, n. 2, p. 241, doi. 10.1002/mds.25188
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- Publication type:
- Article
Erratum to: Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging.
- Published in:
- 2010
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- Publication type:
- Correction notice
Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging.
- Published in:
- Human Genetics, 2010, v. 127, n. 4, p. 441, doi. 10.1007/s00439-009-0782-y
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- Publication type:
- Article
Evidence for statistical epistasis between catechol- O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia.
- Published in:
- Human Genetics, 2007, v. 120, n. 6, p. 889, doi. 10.1007/s00439-006-0257-3
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- Publication type:
- Article
Correction: Stratification and prediction of remission in first-episode psychosis patients: the OPTiMiSE cohort study.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Stratification and prediction of remission in first-episode psychosis patients: the OPTiMiSE cohort study.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-018-0366-5
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- Publication type:
- Article
Epistasis of HTR1A and BDNF risk genes alters cortical 5-HT1A receptor binding: PET results link genotype to molecular phenotype in depression.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-018-0308-2
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- Publication type:
- Article
Effects of a Newly Developed Cognitive Intervention in Amnestic Mild Cognitive Impairment and mild Alzheimer's disease: A Pilot Study.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 25, n. 4, p. 679, doi. 10.3233/JAD-2011-100999
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- Publication type:
- Article
Effects of a newly developed cognitive intervention in amnestic mild cognitive impairment and mild Alzheimer's disease: a pilot study.
- Published in:
- 2011
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- Publication type:
- journal article
Aβ misfolding in blood plasma is inversely associated with body mass index even in middle adulthood.
- Published in:
- Alzheimer's Research & Therapy, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13195-021-00889-2
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- Publication type:
- Article
The Schizophrenia Risk Allele C of the TCF4 rs9960767 Polymorphism Disrupts Sensorimotor Gating in Schizophrenia Spectrum and Healthy Volunteers.
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- Journal of Neuroscience, 2011, v. 31, n. 18, p. 6684, doi. 10.1523/JNEUROSCI.0526-11.2011
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- Publication type:
- Article
Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family-based, Arab-Israeli sample.
- Published in:
- FASEB Journal, 2011, v. 25, n. 11, p. 4011, doi. 10.1096/fj.11-184937
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- Publication type:
- Article
The alternative splicing of tau exon 10 and its regulatory proteins CLK2 and TRA2-BETA1 changes in sporadic Alzheimer's disease.
- Published in:
- Journal of Neurochemistry, 2006, v. 96, n. 3, p. 635, doi. 10.1111/j.1471-4159.2005.03552.x
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- Publication type:
- Article
Patient characteristics, validity of clinical diagnoses and Outcomes Associated with Suicidality in Inpatients with Symptoms of Depression (OASIS-D): design, procedures and outcomes.
- Published in:
- BMC Psychiatry, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12888-023-05230-9
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- Publication type:
- Article
A Ser9Gly Polymorphism in the Dopamine D3 Receptor Gene (DRD3) and Event-Related P300 Potentials.
- Published in:
- Neuropsychopharmacology, 2006, v. 31, n. 6, p. 1335, doi. 10.1038/sj.npp.1300984
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- Publication type:
- Article
Reciprocal moderation by Toxoplasma gondii seropositivity and blood phenylalanine - tyrosine ratio of their associations with trait aggression.
- Published in:
- Pteridines, 2016, v. 27, n. 3/4, p. 77, doi. 10.1515/pterid-2016-0006
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- Publication type:
- Article
In psychiatrically healthy individuals, overweight women but not men have lower tryptophan levels.
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- Pteridines, 2015, v. 26, n. 2, p. 79, doi. 10.1515/pterid-2015-0002
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- Publication type:
- Article
Apolipoprotein E Genotype and the Diagnostic Accuracy of Cerebrospinal Fluid Biomarkers for Alzheimer Disease.
- Published in:
- JAMA Psychiatry, 2014, v. 71, n. 10, p. 1183, doi. 10.1001/jamapsychiatry.2014.1060
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- Publication type:
- Article
Differential Effects of Common Variants in SCN2A on General Cognitive Ability, Brain Physiology, and messenger RNA Expression in Schizophrenia Cases and Control Individuals.
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- JAMA Psychiatry, 2014, v. 71, n. 6, p. 647, doi. 10.1001/jamapsychiatry.2014.157
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- Publication type:
- Article
Penetrance for copy number variants associated with schizophrenia.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3477, doi. 10.1093/hmg/ddq259
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- Publication type:
- Article
Disruption of the neurexin 1 gene is associated with schizophrenia.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 5, p. 988
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- Publication type:
- Article
Strong evidence that GNB1L is associated with schizophrenia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 4, p. 555, doi. 10.1093/hmg/ddm330
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- Publication type:
- Article
Comparison of Extracellular Vesicles from Induced Pluripotent Stem Cell-Derived Brain Cells.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 7, p. 3575, doi. 10.3390/ijms25073575
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- Publication type:
- Article
Coxsackievirus B3 Infection of Human iPSC Lines and Derived Primary Germ-Layer Cells Regarding Receptor Expression.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1220, doi. 10.3390/ijms22031220
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- Publication type:
- Article
Neuronal Stem Cells from Late-Onset Alzheimer Patients Show Altered Regulation of Sirtuin 1 Depending on Apolipoprotein E Indicating Disturbed Stem Cell Plasticity.
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- Molecular Neurobiology, 2024, v. 61, n. 3, p. 1562, doi. 10.1007/s12035-023-03633-z
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- Publication type:
- Article
Common variants conferring risk of schizophrenia.
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- Nature, 2009, v. 460, n. 7256, p. 744, doi. 10.1038/nature08186
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- Publication type:
- Article
Large recurrent microdeletions associated with schizophrenia.
- Published in:
- Nature, 2008, v. 455, n. 7210, p. 232, doi. 10.1038/nature07229
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- Publication type:
- Article
Prescriptions of psychopharmacologic drugs in Austria in 2019 and 2020 – Implications of the COVID-19 pandemic.
- Published in:
- European Psychiatry, 2022, v. 65, n. 1, p. 1, doi. 10.1192/j.eurpsy.2022.2328
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- Publication type:
- Article
A genetic variant within STS previously associated with inattention in boys with attention deficit hyperactivity disorder is associated with enhanced cognition in healthy adult males.
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- Brain & Behavior, 2017, v. 7, n. 3, p. n/a, doi. 10.1002/brb3.646
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- Publication type:
- Article
High-risk Allele for Herpes Labialis Severity at the IFNL3/4 Locus is Associated With Vestibular Neuritis.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.570638
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- Publication type:
- Article
Amyloid blood biomarker detects Alzheimer's disease.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 5, p. 1, doi. 10.15252/emmm.201708763
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- Publication type:
- Article
Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.
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- EMBO Molecular Medicine, 2015, v. 7, n. 12, p. 1565, doi. 10.15252/emmm.201505696
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- Publication type:
- Article
Mild expression differences of MECP2 influencing aggressive social behavior.
- Published in:
- EMBO Molecular Medicine, 2014, v. 6, n. 5, p. 662, doi. 10.1002/emmm.201303744
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- Publication type:
- Article
Az Európai Pszichiátriai Szövetség (European Psychiatric Association, EPA) úmutatója az öngyilkosság kezelésére és megelőzésére.
- Published in:
- Neuropsychopharmacologia Hungarica, 2012, v. 14, n. 2, p. 113, doi. 10.5706/nph201206004
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- Publication type:
- Article
Trehalose as glucose surrogate in proliferation and cellular mobility of adult neural progenitor cells derived from mouse hippocampus.
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- Journal of Neural Transmission, 2019, v. 126, n. 11, p. 1485, doi. 10.1007/s00702-019-02070-4
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- Publication type:
- Article
Childhood adversity and parenting behavior: the role of oxytocin receptor gene polymorphisms.
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- Journal of Neural Transmission, 2019, v. 126, n. 6, p. 777, doi. 10.1007/s00702-019-02009-9
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- Publication type:
- Article
The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits.
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- Journal of Neural Transmission, 2016, v. 123, n. 8, p. 849, doi. 10.1007/s00702-016-1553-2
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- Publication type:
- Article
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease.
- Published in:
- Nature Genetics, 2015, v. 47, n. 5, p. 445, doi. 10.1038/ng.3246
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- Publication type:
- Article
Genome-wide association study identifies five new schizophrenia loci.
- Published in:
- Nature Genetics, 2011, v. 43, n. 10, p. 969, doi. 10.1038/ng.940
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- Publication type:
- Article
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
- Published in:
- Nature Genetics, 2009, v. 41, n. 10, p. 1083, doi. 10.1038/ng.442
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- Publication type:
- Article
Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate.
- Published in:
- 2015
- By:
- Publication type:
- Correction Notice
Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 6, p. 1, doi. 10.1371/journal.pgen.1004345
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- Publication type:
- Article
Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 4, p. 1, doi. 10.1371/journal.pgen.1003455
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- Publication type:
- Article
Neurobiological origins of individual differences in mathematical ability.
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- PLoS Biology, 2020, v. 18, n. 10, p. 1, doi. 10.1371/journal.pbio.3000871
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- Publication type:
- Article
Aβ misfolding in blood plasma measured by immuno-infrared-sensor as an age-independent risk marker of Alzheimer’s disease.
- Published in:
- Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2021, v. 13, n. 1, p. 1, doi. 10.1002/dad2.12151
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- Publication type:
- Article
Methylphenidate Effects on Brain Activity as a Function of SLC6A3 Genotype and Striatal Dopamine Transporter Availability.
- Published in:
- Neuropsychopharmacology, 2015, v. 40, n. 3, p. 736, doi. 10.1038/npp.2014.240
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- Publication type:
- Article